Hemostasis valve orientation relative to the fluid space in a introducer sheath

ABSTRACT

A hemostasis device includes a valve, the valve being sized and configured to be disposed entirely within a handle of medical device, the valve including a rim, the rim be sized and configured to seal with a lumen of the handle of the medical device.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a divisional application of U.S. application Ser.No. 16/781,203, filed Feb. 4, 2020, the entire contents of which areincorporated herein by reference.

FIELD

The present technology is generally related to hemostasis valves forintroducer sheaths.

BACKGROUND

Cardiovascular interventional devices introduced into a given arterialor venous vessel for a variety of purposes, such as cryogenic orradiofrequency ablation, as well as angiographic procedures, have beenknown for many years. Several techniques for introducing such cathetersare available, for example, surgically opening a vein or artery with aneedle, inserting a guide wire into the vein or artery through the lumenof the needle, withdrawing the needle, inserting over the guide wire adilator located inside an associated hemostasis valve and sheath,removing the dilator, and inserting a catheter through the hemostasisvalve and sheath into the blood vessel. In this process, care must beexercised to prevent introduction of air into the vessel and it isdesirable to avoid leakage of blood out of the proximal end of thesheath. To avoid the risk of introducing air into the blood stream,modern introducers for the placement of such interventional devicesemploy various types of hemostasis valves. Such hemostasis valves aredesigned for use with more than one diameter of catheters and guidewires that can be introduced within and through the hemostasis valve andouter sheath for the purposes listed above. However, a risk remains thatair may enter the catheter or sheath, and thus the blood vessel, evenwith current hemostasis valves.

SUMMARY

The techniques of this disclosure generally relate to hemostasis valvesfor steerable sheaths.

In one aspect, a hemostasis device includes a valve, the valve beingsized and configured to be disposed entirely within a handle of medicaldevice, the valve including a rim, the rim be sized and configured toseal with a lumen of the handle of the medical device.

In another aspect of this embodiment, the valve is a disk valve.

In another aspect of this embodiment, the valve includes a valve body,and wherein the valve body defines a first diameter and the rim definesa second diameter larger than the first diameter.

In another aspect of this embodiment, the medical device is anintroducer sheath.

In another aspect of this embodiment, the valve includes a proximalportion configured to be proximate the proximal end of the handle and adistal portion configured to be disposed proximate the proximal end ofthe steerable sheath, and wherein is disposed about the distal portion.

In another aspect of this embodiment, the valve body has a distal mostend, and wherein the rim is proximal to the distal most end andsubstantially orthogonal to the distal most end.

In another aspect of this embodiment, when the valve is disposed withinthe lumen of the handle, the distal most end extends into the lumen.

In another aspect of this embodiment, the rim is a gasket.

In another embodiment, a hemostasis device includes a valve defining asubstantially hyperboloid shape.

In another aspect of this embodiment, the valve includes a first portionsymmetric with a second portion, and wherein the valve first includes aplurality of struts connecting the first portion to the second portion.

In another aspect of this embodiment, the first portion includes a firstend and a second end, the first end having a larger diameter than theproximal end, and the second portion includes a third end and a fourthend, the fourth end includes a larger diameter than then third end, andwherein the second end and the third end each define a plurality ofslits.

In another aspect of this embodiment, the valve is unitary.

In another aspect of this embodiment, the valve is sized to be disposedwithin at least a portion of a handle for a steerable sheath.

In another embodiment, a hemostasis device includes a valve includesfirst substantially toroidal portion and an opposite secondsubstantially toroidal portion.

In another aspect of this embodiment, the valve includes a flangedisposed between the first substantially toroidal portion and the secondsubstantially toroidal portion.

In another aspect of this embodiment, the first substantially toroidalportion includes a first gasket and the second substantially toroidalportion includes a second gasket.

In another aspect of this embodiment, the flange is disposed between thefirst gasket and the second gasket.

In another aspect of this embodiment, the valve is sized to be disposedwithin at least a portion of a handle for a steerable sheath.

In another aspect of this embodiment, the first gasket and the secondgasket each define rings.

In another aspect of this embodiment, the valve is composed of at leastone from the group consisting of polyurethane and silicone.

The details of one or more aspects of the disclosure are set forth inthe accompanying drawings and the description below. Other features,objects, and advantages of the techniques described in this disclosurewill be apparent from the description and drawings, and from the claims.

BRIEF DESCRIPTION OF THE DRAWINGS

A more complete understanding of the present invention, and theattendant advantages and features thereof, will be more readilyunderstood by reference to the following detailed description whenconsidered in conjunction with the accompanying drawings wherein:

FIG. 1 is a perspective view of an exemplary steerable sheath inaccordance with the principles of the present application;

FIG. 2 is cross-sectional view of a proximal portion of the handle ofthe steerable sheath shown in FIG. 1 ;

FIG. 3 is a perspective view of a hemostasis device constructed inaccordance with the principles of the present application;

FIG. 4 is a cross-section view of the hemostasis device shown in FIG. 3;

FIG. 5 is a perspective view of another hemostasis device constructed inaccordance with the principles of the present application;

FIG. 6 is a cross-sectional view of the hemostasis device shown in FIG.5 ;

FIG. 7 is side view of the hemostasis device shown in FIG. 5 ;

FIG. 8 is a perspective view of another hemostasis device constructed inaccordance with the principles of the present application;

FIG. 9 is a view of a first portion of the hemostasis device shown inFIG. 8 ;

FIG. 10 is side view of the hemostasis device shown in FIG. 8 ;

FIG. 11 is a cross-sectional view of the hemostasis device shown in FIG.8 ;

FIG. 12 is another embodiment of the hemostasis device shown in FIG. 3 ;and

FIG. 13 is a cross-sectional view of the hemostasis device shown in FIG.12 .

DETAILED DESCRIPTION

It should be understood that various aspects disclosed herein may becombined in different combinations than the combinations specificallypresented in the description and accompanying drawings. It should alsobe understood that, depending on the example, certain acts or events ofany of the processes or methods described herein may be performed in adifferent sequence, may be added, merged, or left out altogether (e.g.,all described acts or events may not be necessary to carry out thetechniques). In addition, while certain aspects of this disclosure aredescribed as being performed by a single module or unit for purposes ofclarity, it should be understood that the techniques of this disclosuremay be performed by a combination of units or modules associated with,for example, a medical device.

Referring now to the drawings in which like reference designators referto like elements, there is shown in FIG. 1 an exemplary medical deviceconstructed in accordance with the principles of the present applicationand designated generally as “10.” The medical device 10 may be asteerable sheath such as Medtronic's Flexcath® devices for use withcardiovascular interventions. In other configurations, the medicaldevice 10 may be any medical device. In the configuration shown in FIG.1 , the medical device 10 includes a handle 12, a sheath 14 extendingfrom the handle 12 and an actuator 16 configured to articulate thesheath 14 such that it can navigate the tortuous pathways of thevasculature.

Referring now to FIG. 2 , the medical device 10 may further includelumen 18 in which a proximal end 20 of the sheath 14 is disposed. Forexample, the proximal end 20 of the sheath 14 may be disposed proximatean opening 21 within the handle 12 that allows another medical device,such as catheter (not shown) to be advanced into the handle 12 and intothe sheath 14. To prevent air or other fluids such as blood fromentering the sheath 14 during the inserting of the catheter, ahemostasis device 22 is at least partially disposed within the lumen 18and entirely disposed within the handle 12. In an exemplaryconfiguration, the hemostasis device 22 is valve 24 composed of, forexample, a thermoplastic elastomer, silicone, or other rubbers. Thehandle 12 may provide a compressive force on the hemostasis device 22,for example, by a friction fit to provide for proper placement andfunction of the hemostasis device 22 such that air is not introducedinto the introducer sheath 14.

Referring now to FIGS. 2-4 , the valve 24 includes a rim 26 sized andconfigured to seal with the lumen 18 of the handle 14 of the medicaldevice 12. For example, the valve 24 may include a valve body 28 whichdefines a first diameter 30. The rim 26 defines a second diameter 32larger than the first diameter 30 and surrounds the valve body 28. Inone configuration, the rim 26 is a gasket. In the configuration shown inFIG. 2 , the rim 26 defines a perpendicular angle with the innerdiameter of the lumen 18 and is substantially flush with the innerdiameter of the lumen 18 when the valve 24 is disposed within the handle12. In another configuration, the inner diameter of the lumen 18 issubstantially co-planar with a distal most end 34 of the valve body28.That is, the lumen 18 rest on the distal most end 34 of the valve body28 and the rim is perpendicular to the distal most end 34 of the valvebody 28. In an exemplary configuration, the valve body 28 is disposedproximate the opening 21 of the handle 12 and the rim 26 is disposedproximate the proximal end 20 of the sheath 14. This valve's 24orientation within the sheath 14 prevents air from entering the sheath14 and blood from leaking out of the sheath 14.

Referring now to FIGS. 5-7 , in another configuration, the hemostasisdevice 22 is valve 36. Valve 36 may be sized and configured to beentirely disposed within the handle 12 of device 10 and at leastpartially disposed within the lumen 18 of the handle 12. Valve 36 may beunitary valve defining a substantially hyperboloid shape, i.e. anhour-glass shape. As shown in FIG. 5 , valve 36 may include a firstportion 38, which may be conical or substantially conical, disposedwithin a valve body 40. The first portion 38 may include a rim 42 sizedand configured to engage lumen 18 of device 10 as discussed above. Thefirst portion 38 may further define a plurality of slits 44 at a distalend of the first portion to facilitate the introduction of a catheter orother device through the valve. The slits 44 may be tricuspid slits, orany other slit geometry configured to allow a device such a catheter topass through. In another configuration, the valve 36 may include thefirst portion 38 symmetric with a second portion 46, which coupledtogether. The first portion 38 and the second portion 46 may each definethe same or similar conical geometry and include respective slits 44facing each other as shown in FIG. 7 . Optionally, a plurality of struts48 radially disposed about the valve 36 configured to providelongitudinal support to the first portion 38 and/or second portion 46,depending on the configuration. Any number of struts 48 may be includedand they may extend into the interior of the valve 36. For example, asshown in FIGS. 6 and 7 , the struts 48 extend toward the interior of thevalve 36 and extend between the rim 42 of the first portion 38 and therim 42 of the second portion 46.

Referring now to FIGS. 8-11 , in another configuration, the hemostasisdevice 22 is a valve 50. Valve 50 may include a first substantiallytoroidal, or doughnut shaped, portion 52 defining a plurality of slits54, for example, tricuspid slits, (shown in FIG. 9 ) for passage of acatheter or other medical device. The valve may include a rim 56 similarto the rims disclosed above configured to engage the lumen 18 of the ofthe device 10 as discussed above. The valve 50 may be unitary or it mayinclude a second substantially toroidal portion 58 symmetric andopposite with the first substantially toroidal portion 52. The firstsubstantially toroidal portion 52 and the second substantially toroidalportion 58 may each define the same or similar geometry and includerespective slits 54 facing each other as shown in FIG. 11 .

Referring now to FIGS. 12-13 , in another configuration of the valve 24shown in FIG. 3 , valve 60 may include a valve body 62, and furtherinclude a rim 64 sized and configured to seal with the lumen 18 of thehandle 12 of the medical device 12. However, in this configuration, thevalve body 64 tapers in a curved manner toward the slits 66, as opposedto a straight taper as shown in FIG. 4 .

It will be appreciated by persons skilled in the art that the presentinvention is not limited to what has been particularly shown anddescribed herein above. In addition, unless mention was made above tothe contrary, it should be noted that all of the accompanying drawingsare not to scale. A variety of modifications and variations are possiblein light of the above teachings without departing from the scope andspirit of the invention, which is limited only by the following claims.

What is claimed is:
 1. A hemostasis device, comprising: a valveincluding a first substantially toroidal portion and an opposite secondsubstantially toroidal portion.
 2. The device of claim 1, wherein thevalve includes a flange disposed between the first substantiallytoroidal portion and the second substantially toroidal portion.
 3. Thedevice of claim 2, wherein the first substantially toroidal portionincludes a first gasket and the second substantially toroidal portionincludes a second gasket.
 4. The device of claim 3, wherein the flangeis disposed between the first gasket and the second gasket.
 5. Thedevice of claim 4, wherein the valve is sized to be disposed within atleast a portion of a handle for a steerable sheath.
 6. The device ofclaim 4, wherein the first gasket and the second gasket each definerings.
 7. The device of claim 6, wherein the valve is composed of atleast one from the group consisting of polyurethane and silicone.